Evidence map›Paper›PMID 29086247›Full record

ArticleMolecular neurobiology2018

Paracrine and Intracrine Angiotensin 1-7/Mas Receptor Axis in the Substantia Nigra of Rodents, Monkeys, and Humans.

Maria A Costa-Besada, Rita Valenzuela, Pablo Garrido-Gil, Begoña Villar-Cheda, Juan A Parga, Jose L Lanciego, Jose L Labandeira-Garcia

Open access · bronzeAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
  2. Article
  3. Ang II-mediated effects on BBB integrity in psychiatric and neurological disorders.Progress in neuro-psychopharmacology & biological psychiatry · 2026
    Review
  4. Microglial activation and RAS signaling: a dual-edged sword in neuroinflammation.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
    Review
  5. Review
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  10. Article
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  19. Altered Gene Expression Within the Renin-Angiotensin System in Normal Aging and Dementia.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Maria A Costa-BesadaLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Rita ValenzuelaLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Pablo Garrido-GilLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Begoña Villar-ChedaLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Juan A PargaLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Jose L LanciegoNetworking Research Center on Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Jose L Labandeira-GarciaLaboratory of Neuroanatomy and Experimental Neurology, Dept. of Morphological Sciences, CIMUS, Faculty of Medicine, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain. joseluis.labandeira@usc.es.
Biomedical Research Networking Center on Neurodegenerative Diseases · ESUniversidade de Santiago de Compostela · ESUniversidad de Navarra · ES

Funding

Galician Government (XUGA) GRC2014/002; CIMUS accreditation 2016-2019, ED431G/05Spanish Ministry of Economy and Competitiveness BFU2015-70523Spanish Ministry of Health RD12/0019/0020, RD16/0011/0016
6 · The paper itself

Abstract

In addition to the classical hormonal (tissue-to-tissue) renin-angiotensin system (RAS), there are a paracrine (cell-to-cell) and an intracrine (intracellular/nuclear) RAS. A local paracrine brain RAS has been associated with several brain disorders, including Parkinson's disease (PD). Classically, angiotensin II (Ang II) is the main RAS effector peptide and acts through two major receptors: Ang II type 1 and 2 (AT1 and AT2) receptors. It has been shown that enhanced activation of the Ang II/AT1 axis exacerbates dopaminergic cell death. Several new components of the RAS have more recently been discovered. However, the role of new Ang 1-7/Mas receptor RAS component was not investigated in the brain and particularly in the dopaminergic system. In the present study, we observed Mas receptor labeling in dopaminergic neurons and glial cells in rat mesencephalic primary cultures; substantia nigra of rats, monkeys, and humans; and human induced pluripotent stem (iPS) cells derived from healthy controls and sporadic PD patients. The present data support a neuroprotective role of the Ang 1-7/Mas receptor axis in the dopaminergic system. We observed that this axis is downregulated with aging, which may contribute to the aging-related vulnerability to neurodegeneration. We have also identified an intracellular Ang 1-7/Mas axis that modulates mitochondrial and nuclear levels of superoxide. The present data suggest that nuclear RAS receptors regulate the adequate balance between the detrimental and the protective arms of the cell RAS. The results further support that the brain RAS should be taken into account for the design of new therapeutic strategies for PD.

Indexed as

Paracrine CommunicationSignal TransductionAgingAngiotensin IAngiotensin IIAnimalsAstrocytesCase-Control StudiesCell NucleusCells, CulturedDopaminergic NeuronsGene DeletionHaplorhiniMaleMesencephalonMicrogliaAngiotensin Iangiotensin I (1-7)Angiotensin IIPeptide FragmentsPeptidyl-Dipeptidase AProto-Oncogene MasProto-Oncogene ProteinsReactive Nitrogen SpeciesReactive Oxygen SpeciesReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Receptors, G-Protein-CoupledAgingDopaminergicNeuroprotectionNuclear receptorsParkinson’s diseaseRenin-angiotensin system

Identifiers

PMID29086247
PMCPMC7102204
OpenAlexW2765096292

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.